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Preparations of buffers

Dilute 10 times with distilled water before use [Pg.29]

Citrate buffer for heat-induced antigen retrieval [Pg.29]


The method of preparation of buffer solutions with the certain acidity value from HMTA and HCl aqueous solutions is offered. It is recommended to use the equations ... [Pg.38]

What is the Henderson-Hasselbalch equation Tell how it is useful in the preparation of buffer... [Pg.141]

Preparation of buffers with the same ionic strength... [Pg.66]

Click on Buffers. Review Preparation of Buffers, Definitions of pH, Hender-son-Hasselbalch Equation and Buffer Calculator. [Pg.58]

This section describes the preparation of buffers and reagents used in the manipulation of nucleic acids. [Pg.1311]

Reagents. Cyclic nucleotides (3, 5 -cyclic adenosine monophosphate (c-AMP), 3, 5 -cyclic guanosine monophosphate (c-GMP), and 3, 5 -cyclic inosine monophosphate (c-IMP)) sodium tetraborate hydrochloric acid and potassium hydroxide were purchased from Sigma Chemical Company, St. Louis, Missouri). Millex disposable filter units (0.22 pm) were obtained from Millipore Corporation (Bedford, Massachusetts). Triply distilled and deionized water was used for the preparation of buffer solutions. Both buffers and samples were routinely degassed with helium after filtration (using microfilter units). [Pg.52]

Preparation of Buffers containing TFA (0.1% v/v) for Analytical HPLC SP0511 ... [Pg.125]

Preparation of Buffer of Known pH and Strength Given 0.10 m solutions of acetic acid (pKa = 4.76) and sodium acetate, describe how you would go about preparing 1.0 L of 0.10 M acetate buffer of pH 4.00. [Pg.20]

The isolation of human hepatocytes is described according to Hengstler et al. (Hengstler 2000). Preparation of buffer solutions ... [Pg.506]

It is unfortunate that there has been so little work devoted to quantitative measurements of cation-pseudobase equilibria in methanol and ethanol since these media have several advantages over water for the determination of the relative susceptibilities of heterocyclic cations to pseudobase formation. The enhanced stability of the pseudobase relative to the cation in alcohols compared to water is discussed earlier this phenomenon will permit the quantitative measurement of pseudobase formation in methanol (and especially ethanol) for many heterocyclic cations for which the equilibrium lies too far in favor of the cation in aqueous solution to allow a direct measurement of the equilibrium constant. Furthermore, the deprotonation of hydroxide pseudobases (Section V,B) and the occurrence of subsequent irreversible reactions (Sections V,C and D), which complicate measurements for pKR+ > 14 in aqueous solutions, are not problems in alcohol solutions. Data are now available for the preparation of buffer solutions in methanol over a wide range of acidities.309-312 An appropriate basicity function scale will be required for more basic solutions. The series of -(substituted phenyl)pyridinium cations (163) studied by Kavalek et al.i2 should be suitable for use as indicators in at least some of the basic region. The Hm and Jm basicity functions313 should not be assumed90 to apply to methoxide ion addition to heterocyclic cations because of the differently charged species involved in the indicators used to construct these scales. [Pg.66]

Preparation of Buffer Solutions.—The buffer capacity of a given acid-base system is a maximum, according to equation (77), when there are present equivalent amounts of acid and salt the hydrogen ion concentration is then equal to and the pH is equal to pfca. If the ratio of acid to salt is increased or decreased ten-fold, i.e., to 10 1 or 1 10, the hydrogen ion concentration is then lOfca or O.IAto, and the pH is pA a — 1 or pfca + 1, respectively. If these values for cn are inserted in equation (76), it is found that the buffer capacity is then... [Pg.413]

For details concerning the preparation of buffer solutions, see Clark, The Determination of Hydrogen Ions, 1928, Chap. IX Britton, Hydrogen Ions, 1932, Chap. XI Kolthoff and Rosenblum, Acid-Base Indicators, 1937, Chap. VIII. [Pg.414]

Tris is short for tris(hydroxymethyl)aminomethane. This weak base is widely used in biochemical research for the preparation of buffers. It offers low toxicity and a pK, (5.92 at 25°C) that is convenient for the control of pH in clinical applications. A buffer is prepared by mixing 0.050 mol of tris with 0.025 mol of HCl in a volume of 2.00 L. Compute the pH of the solution. [Pg.671]

The Common Ion Effect and Buffer Solutions 19-2 Buffering Action 19-3 Preparation of Buffer Solutions 19-4 Acid-Base Indicators... [Pg.793]


See other pages where Preparations of buffers is mentioned: [Pg.940]    [Pg.178]    [Pg.1284]    [Pg.1337]    [Pg.1209]    [Pg.4]    [Pg.862]    [Pg.201]    [Pg.29]    [Pg.1045]    [Pg.548]    [Pg.552]    [Pg.553]    [Pg.555]    [Pg.557]    [Pg.559]    [Pg.279]    [Pg.201]    [Pg.650]    [Pg.212]    [Pg.23]    [Pg.61]    [Pg.39]    [Pg.90]    [Pg.87]    [Pg.329]    [Pg.220]    [Pg.258]    [Pg.803]    [Pg.803]    [Pg.803]    [Pg.804]    [Pg.805]   


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